Evidence map›Paper›PMID 33216887›Full record

Trial reportBlood advances2020

Virus-specific T-cell therapy to treat BK polyomavirus infection in bone marrow and solid organ transplant recipients.

Adam S Nelson, Daria Heyenbruch, Jeremy D Rubinstein, Anthony Sabulski, Sonata Jodele, Shawn Thomas, Carolyn Lutzko, Xiang Zhu, Thomas Leemhuis, Jose A Cancelas and 5 more

2 registry-linked trialsOpen access · greenAbstract readClinical Trial
In one paragraph

Trial report in Blood advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.7field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT02532452 phase2recruitingnot on this map

Third Party Viral Specific T-cells (VSTs) for Treatment of Viral Infections in Immunocompromised Patients

TypeinterventionalSponsorChildren's Hospital Medical Center, CincinnatiRan2015 to 2027Enrolled750ConditionsViral Infection, Viral Reactivation, Infection in an Immunocompromised HostArmsViral Specific VST Infusion
NCT07685457 narecruitingnot on this mapstarted 2026, after this paper: background citation

A Prospective Clinical Study to Evaluate the Safety and Efficacy of Virus Specific T-Cell Administration in Pediatric Patients With Systemic Viral Infection Following Allogeneic Hematopoietic Stem Cell Transplantation.

TypeinterventionalSponsorLucasBioRan2026 to 2027Enrolled6ConditionsBKV Infection, CMV Infection, EBV InfectionArmsLB-DTK-MV
3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 75 citations in OpenAlex.

  1. Trial
  2. Posoleucel, an Allogeneic, Off-the-Shelf Multivirus-Specific T-Cell Therapy, for the Treatment of Refractory Viral Infections in the Post-HCT Setting.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
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  6. Review
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  9. Adoptive T-cell therapy for virus-associated diseases.Clinical microbiology reviews · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 3 institutions in 1 country.

Adam S NelsonDivision of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, OH.
Daria HeyenbruchHoxworth Blood Center, Cincinnati, OH.
Jeremy D RubinsteinDivision of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, OH.
Anthony SabulskiDivision of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, OH.
Sonata JodeleDivision of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, OH.
Shawn ThomasDivision of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, OH.
Carolyn LutzkoExperimental Hematology and Cancer Biology, Cincinnati Children's Hospital, Cincinnati, OH; and.
Xiang ZhuExperimental Hematology and Cancer Biology, Cincinnati Children's Hospital, Cincinnati, OH; and.
Thomas LeemhuisHoxworth Blood Center, Cincinnati, OH.
Jose A CancelasHoxworth Blood Center, Cincinnati, OH.
Michael KellerProgram for Cell Enhancement and Technologies for Immunotherapy, Children's National Health System and The George Washington University, Washington, DC.
Catherine M BollardProgram for Cell Enhancement and Technologies for Immunotherapy, Children's National Health System and The George Washington University, Washington, DC.
Patrick J HanleyProgram for Cell Enhancement and Technologies for Immunotherapy, Children's National Health System and The George Washington University, Washington, DC.
Stella M DaviesDivision of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, OH.
Michael S GrimleyDivision of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children's Hospital, Cincinnati, OH.
Cincinnati Children's Hospital Medical Center · USGeorge Washington University · USUniversity of Cincinnati Medical Center · US

Funding

Thrombotic microangiopathy (TMA) associated MODS after stem cell transplantationR01HD093773 · NICHD · CINCINNATI CHILDRENS HOSP MED CTR · PI JODELE, SONATA · 2018 to 2021
$2.8M
NICHD NIH HHS R01 HD093773
6 · The paper itself

Abstract

BK polyomavirus (BKPyV) infection is a major complication of hematopoietic stem cell transplant (HSCT) and solid organ transplant (SOT). Treatment options are limited, poorly effective, and have significant toxicities. Cellular therapy using T cells directed against BKPyV is an emerging therapy, and we report efficacy in controlling BKPyV-associated disease in highly immunocompromised patients. Virus-specific T cells (VSTs) against BKPyV were manufactured using either blood from the patient's stem cell donor (donor-derived VSTs) or from unrelated donors (third-party VSTs). VSTs were used to treat BKPyV in 38 HSCT recipients and 3 SOT recipients between June 2017 and December 2019. Overall response rate was 86% in patients treated for BK viremia, 100% in patients treated for hemorrhagic cystitis, and 87% in patients treated for both BK viremia and hemorrhagic cystitis. No infusional toxicity, de novo graft-versus-host disease, or rejection of the organ occurred attributable to the VST infusion. BKPyV-specific immune responses were demonstrated by interferon-γ production by peripheral blood mononuclear cells postinfusion in response to BKPyV antigens. VSTs are a safe and potentially effective strategy to treat BKPyV and associated symptoms in recipients of HSCT and SOT. Cellular therapy should be considered for all patients with BKPyV and underlying immune suppression at risk of complications. This trial was registered at www.clinicaltrials.gov as #NCT02532452.

Indexed as

BK VirusPolyomavirus InfectionsBone MarrowCell- and Tissue-Based TherapyHumansLeukocytes, Mononuclear

Identifiers

PMID33216887
PMCPMC7686882
OpenAlexW3099917553

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.